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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390602Generated: November 4, 2026

Hydrochloric Acid → 2,4-Dichloro-alpha-(chloromethyl)benzenepropanol

https://huagongshe.com/reaction/1390602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,4-Dichlorobenzyl chlorideHCID 7212—
ReactantEpichlorohydrinHCID 7835—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product2,4-Dichloro-alpha-(chloromethyl)benzenepropanolHCID 20476872—

Reaction Steps

To a stirred and refluxing Grignard-complex, previously prepared starting from 98 parts of 1-(chloromethyl)-2,4-dichlorobenzene and 14 parts of magnesium in 70 parts of 1,1-oxybisethane, is added dropwise a solution of 46.5 parts of 2-(chloromethyl)oxirane in 350 parts of 1,1'-oxybisethane. Upon completion, stirring at reflux temperature is continued overnight. The reaction mixture is cooled in an ice-bath and decomposed by dropwise addition of 120 parts of a concentrated hydrochloric acid solution. The whole is poured onto water and the layers are separated. The organic phase is washed three times with water. The aqueous phase is extracted with 1,1'-oxybisethane. The combined organic phases are dried, filtered and evaporated. The residue is distilled, yielding 2,4-dichloro-α-(chloromethyl)benzenepropanol; bp. 130° C. at 0.04 mm. pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04139540
Source datasetuspto-grants-1979_02
ORD IDord-a7550d53dba14c3a9ad28f6a35d02bba
Source noteuspto-grants-1979_02